Milvexian for the Prevention of Venous Thromboembolism

被引:159
|
作者
Weitz, Jeffrey, I [1 ,2 ]
Strony, John [3 ]
Ageno, Walter [4 ]
Gailani, David [5 ]
Hylek, Elaine M. [6 ]
Lassen, Michael R. [7 ]
Mahaffey, Kenneth W. [8 ]
Notani, Ravi S. [3 ]
Roberts, Robin [1 ,2 ]
Segers, Annelise [9 ]
Raskob, Gary E. [10 ]
机构
[1] Thrombosis & Atherosclerosis Res Inst, 237 Barton St East, Hamilton, ON L8L 2X2, Canada
[2] McMaster Univ, Hamilton, ON, Canada
[3] Janssen Res & Dev, Raritan, NJ USA
[4] Univ Insubria, Varese, Italy
[5] Vanderbilt Univ, Med Ctr, Nashville, TN USA
[6] Boston Univ, Sch Med, Boston, MA 02118 USA
[7] Gildhoj Private Hosp, Copenhagen, Denmark
[8] Stanford Univ, Dept Med, Sch Med, Stanford Ctr Clin Res, Stanford, CA 94305 USA
[9] Int Trial Expertise Advisory & Serv, Amsterdam, Netherlands
[10] Univ Oklahoma, Hlth Sci Ctr, Hudson Coll Publ Hlth, Oklahoma City, OK USA
来源
NEW ENGLAND JOURNAL OF MEDICINE | 2021年 / 385卷 / 23期
关键词
FACTOR-XI DEFICIENCY;
D O I
10.1056/NEJMoa2113194
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND Factor XIa inhibitors for the prevention and treatment of venous and arterial thromboembolism may be more effective and result in less bleeding than conventional anticoagulants. Additional data are needed regarding the efficacy and safety of milvexian, an oral factor XIa inhibitor. METHODS In this parallel-group, phase 2 trial, we randomly assigned 1242 patients undergoing knee arthroplasty to receive one of seven postoperative regimens of milvexian (25 mg, 50 mg, 100 mg, or 200 mg twice daily or 25 mg, 50 mg, or 200 mg once daily) or enoxaparin (40 mg once daily). The primary efficacy outcome was venous thromboembolism (which was a composite of asymptomatic deep-vein thrombosis, confirmed symptomatic venous thromboembolism, or death from any cause). The principal safety outcome was bleeding. RESULTS Among the patients receiving milvexian twice daily, venous thromboembolism developed in 27 of 129 (21%) taking 25 mg, in 14 of 124 (11%) taking 50 mg, in 12 of 134 (9%) taking 100 mg, and in 10 of 131 (8%) taking 200 mg. Among those receiving milvexian once daily, venous thromboembolism developed in 7 of 28 (25%) taking 25 mg, in 30 of 127 (24%) taking 50 mg, and in 8 of 123 (7%) taking 200 mg, as compared with 54 of 252 patients (21%) taking enoxaparin. The dose-response relationship with twice-daily milvexian was significant (one-sided P<0.001), and the 12% incidence of venous thromboembolism with twice-daily milvexian was significantly lower than the prespecified benchmark of 30% (one-sided P<0.001). Bleeding of any severity occurred in 38 of 923 patients (4%) taking milvexian and in 12 of 296 patients (4%) taking enoxaparin; major or clinically relevant nonmajor bleeding occurred in 1% and 2%, respectively; and serious adverse events were reported in 2% and 4%, respectively. CONCLUSIONS Postoperative factor XIa inhibition with oral milvexian in patients undergoing knee arthroplasty was effective for the prevention of venous thromboembolism and was associated with a low risk of bleeding.
引用
收藏
页码:2161 / 2172
页数:12
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